Superoxide Radical Scavenging Research Articles

Assessment of Antioxidant and Scavenging Activities of Various Yogurts Using Different Sample Preparation Procedures

Antioxidant activities of various yogurts were assessed using different sample preparation procedures. Specifically, full-fat cow, goat and ewe yogurts as well as cow yogurts with different fat content (4%, 2% and 0%) were employed. Antioxidant activities were determined in two different water-soluble yogurt extracts and also in a total yogurt preparation using the “Clarifying Reagent” for dairy products. Full-fat ewe yogurt preparations exhibited higher antioxidant activities in FRAP and Folin assays as well as higher scavenging capacities against DPPH, hydroxyl and superoxide anion radicals than full-fat cow and goat yogurt preparations. Bradford, Lowry and Ellman’s assays confirmed that the strong antioxidant potential of the ewe yogurt was associated with its high protein content. In addition, antioxidant activities appeared to be related with the fat content of cow yogurt. Particularly, in DPPH, FRAP and Folin assays, and also in assays for scavenging of DPPH, hydroxyl and superoxide anion radicals, it was demonstrated that the fat removal led to the increase of the antioxidant/scavenging activities of the cow yogurts due to the increase of their protein/peptide water-soluble content. Moreover, for the first time, results show that the “Clarifying Reagent” for dairy products can be used for the determination of antioxidant and radical scavenging activities of whole yogurt using the FRAP assay as well as the hydroxyl and superoxide anion radicals scavenging assays.

Preparation and antioxidant activity of novel chitosan oligosaccharide quinolinyl urea derivatives

In the present study, four new chitosan oligosaccharide derivatives bearing quinolinyl urea groups were synthesized by reaction between 2-methoxyformylated chitosan oligosaccharide and aminoquinoline. The chitosan oligosaccharide derivatives were characterized by Fourier Transform Infrared (FTIR) and 1H Nuclear Magnetic Resonance (1H NMR) spectroscopy. The obtained results confirmed that chitosan oligosaccharide quinolinyl urea derivatives were successfully synthesized. Meanwhile, the antioxidant activities of different chitosan oligosaccharide derivatives were examined in vitro. Experimentally, it was demonstrated that chitosan oligosaccharide quinolinyl urea derivatives had superior antioxidant activity compared with chitosan oligosaccharide and the antioxidant effects were concentration-dependent. Especially, when the concentration was 1.6 mg/mL, their superoxide anion radical scavenging rates could reach to 72.35 ± 0.49%, 100.00 ± 0.21%, 84.63 ± 0.49%, and 87.22 ± 0.32%, respectively. And the hydroxyl radical scavenging rates could reach to 100.00 ± 0.82%, 98.49 ± 4.08%, 100.00 ± 5.76%, and 92.07 ± 5.10%. In addition, the cytotoxic activity of the prepared chitosan derivatives against L929 cells was determined by CCK-8 assay. The cell survival rates were all higher than 90%, which intuitively indicated that the samples had almost no cytotoxicity. The findings indicated that the enhanced antioxidant property and biocompatibility of these chitosan oligosaccharide quinolinyl urea derivatives could enlarge the scope of the application of chitosan oligosaccharide, particularly as an antioxidant in food packaging, biomedical, pharmaceutical, cosmetics industries and other fields.

Evaluation of phytochemical content and in vitro antioxidant properties of methanol extract of Allium cepa, Carica papaya and Cucurbita maxima blossoms

Antioxidants are helpful in offering resistance against high production of free radicals in the body because of their ability to donate electrons that can neutralize the radical formation. This study identified and quantified the in vitro antioxidant and polyphenolic content from methanol extracts of three commonly available edible flowers of Allium cepa, Carica papaya and Cucurbita maxima by using several standardized antioxidant assay methods. The flowers were chosen as unconventional, yet an easily available source of potential nutritive value. Amongst the three flowers, at 500 µg/ml concentration in Ferric Thiocyanate (FTC) assay method, the methanol extract of Carica papaya showed better scavenging activity with the lowest IC50 of 17.47 µg/ml followed by Allium cepa umbel with IC50 of 37.06 µg/ml and Cucurbita maxima flowers in Superoxide radical scavenging assay at 500 µg/ml with IC50 of 56.06 µg/ml. Phytochemical analysis revealed the presence of higher quantity of phenols than flavonoids in the three flowers. Carica papaya recorded the highest amount of phenol content (108.66 mg GAE/100 g) and Cucurbita maxima with a slightly higher quantity of flavonoids (17.2 mg QE/100 g) which correlated with its antioxidant activity. It can be concluded that these flowers possess alleviating properties against reactive oxygen species-induced damage.

The design, synthesis, antioxidant, and antihypoxia activities of two new hydroxydaidzein derivatives

7,8,3’,4’,5’-Pentahydroxyisoflavone (8,3’,5’-trihydroxydaidzein) and 6,7,8,3’,4’,5’-hexahydroxyisoflavone (6,8,3’,5’-tetrahydroxydaidzein) are synthesized via a simple and effective method using commercially available daidzein as a raw material. Their structures are confirmed using spectroscopic analyses (infrared, nuclear magnetic resonance, and mass spectrometry), and their purities are determined by high-performance liquid chromatography. The antioxidant capacities are investigated by utilizing 1,1-diphenyl-2-picryl-hydrazyl radical scavenging, superoxide radical scavenging, nitric oxide radical scavenging, reducing power, and phosphomolybdenum assays. The antihypoxia activity is examined using a hypoxia-induced PC12 cell injury model. The antioxidant and antihypoxia abilities of 8,3’,5’-trihydroxydaidzein and 6,8,3’,5’-tetrahydroxydaidzein are greatly improved in comparison with daidzein. These results indicate that 8,3’,5’-trihydroxydaidzein and 6,8,3’,5’-tetrahydroxydaidzein are excellent antioxidant agents and can be used for alleviating injury induced by hypoxia.

Appraisal of Antioxidant Potential of Saussurea lappa and Valeriana wallichii Root Extract by In-vitro Techniques

>Background: Antioxidants are very important in preventing and protecting from oxidative stress and, ultimately, oxidative stress-related disorders. With the aim to the antioxidant activity of Saussurea lappa and Valeriana wallichii extract, individually and in combination, the study was performed via assays for antioxidant capability; 1, 1-diphenyl-2-picrylhydrazyl radical (DPPH), nitric oxide scavenging method, ferric reducing antioxidant power (FRAP), H2O2 scavenging potential, superoxide radical scavenging method showed good antioxidant activity. Individually, V. wallichii having more superior antioxidant activity than S. lappa. Results: Phytochemical analysis of both extracts individually illustrate the existence of anthraquinones, cardiac glycoside, flavonoids, reducing sugars, phenolics, saponins, alkaloid terpenoids, and phlobatannin. In combination, the antioxidant activity was improved, indicating additive effects. The results indicate that these herbs can be a very good constituent for combination therapy for diseases that are caused by oxidative stress and require antioxidant therapy. The S. lappa and V. wallichii showed average TPC of 68.38 and 117.52 mg GAE/g of extract, respectively. The mix of 1:1 ratio of both extracts showed TPC of 101.34 mg GAE/g. The S. lappa and V. wallichii showed average TFC of 59.72 and73.56 mg QE/g of extract, respectively. The mix of 1:1 ratio of both extracts showed a TFC of 66.15 mg QE/g of extract. Results showed that both extracts have very strong antioxidant activity. V. wallichii has relatively higher antioxidant activity and is close to that of ascorbic acid.

Phytochemical Analysis and Evaluation of Antimicrobial, Antioxidant, Anti-inflammatory and Antiangiogenic activities of Methanol extract of Urochloa ramosa

Urochloa ramosa is a plant of the wet, seasonally dry and semi-arid tropics. It is also known as Bracharia ramosa or Brown top millet. Qualitative analysis of phytochemicals in methanol extracts were performed by standard methods. Partially purified phenolics from the methanol extract of leaf sample was subjected for different biological activities. In vitro antimicrobial activity was executed on Bacillus subtilis, Staphylococcus epidermidis and Staphylococcus aureus (Gram positive) and Proteus, Salmonella and Escherichia coli (Gram negative) bacteria and Candida albicans (yeast type fungi). Minimum inhibitory concentration was calculated by Resazurin method. In-vitro antioxidant assay was conducted by DPPH radical, NO. radical, superoxide anion radical scavenging assays and OH radical scavenging activity by DNA protection assay using BHT as the reference compound. IC50 value of methanol extract for each of these assays was calculated. Albumin denaturation assay, antiproteinase activity and membrane stabilization were performed to test the anti-inflammatory potential at various concentrations of methanol extract of U.ramosa. In vivo anti-angiogenesis activity was carried out by shell less chick chorioallantoic membrane assay. In the antimicrobial activity we found that Staphylococcus aureus showed considerable susceptiblity with the MIC value of 145μg and Staphylococcus epidermidis is the most resistant with the MIC value of 378μg/ml. IC50 of 10.10µg/ml, IC50 of 17.32µg/ml and IC50 of 25.12µg/ml demonstrated antioxidant activities of methanol extract of U. ramosa by scavenging DPPH, NO. and superoxide anion radicals respectively. At 100µg/ml concentration, methanol extract significantly protected DNA against the effect of hydroxyl radicals. Protein denaturation was protected between concentrations 100-500µg/ml of methanol extract, maximum proteinase inhibitory activity was significantly found at 500µg/ml concentration and even haemolysis (heat and hypotonicity induced) was prevented considerably at 500µg/ml of methanol extract. Inhibition of proliferation of capillaries was observed in chorioallantoic membrane assay proving methanol extract’s antiangiogenic property. The leaves of Urochloa ramosa are basically enriched with natural phenolics with multitudinous biological potencies that can represent a promising class as bioactive molecules.

Exopolymer-Functionalized Nanoselenium from Bacillus subtilis SR41: Characterization, Monosaccharide Analysis and Free Radical Scavenging Ability.

To provide a safe and effective supplement of the essential trace element selenium, we focused on the biosynthesis of nanoselenium (SeNPs) via probiotics. A novel kind of exopolymer-functionalized nanoselenium (SeEPS), whose average size was 67.0 ± 0.6 nm, was produced by Bacillus subtilis SR41, whereas the control consisted of exopolymers without selenium (EPS). Chemical composition analysis, Fourier transform infrared (FTIR) spectroscopy and high-performance liquid chromatography (HPLC) confirmed that SeEPS and EPS shared similar polysaccharide characteristic groups, such as COO- and C=O, and contained not only 45.2–45.4% of sugars but also 23.5–24.7% of proteins and some lipids. Both SeEPS and EPS were primarily composed of mannose, amino glucose, ribose, glucose and galactose. Furthermore, to identify the biologically active component of SeEPS, three kinds of selenium particles with different stabilizers [Se(0), bovine serum albumin-Se and EPS-Se] were synthesized chemically, and their ability to scavenge free radicals in vitro was compared with that of SeEPS and EPS. The results revealed that EPS itself exhibited weak superoxide and hydroxyl radical scavenging abilities. Nevertheless, SeEPS had superior antioxidant properties compared to all other products, possibly due to the specific structure of SeNPs and exopolymers. Our results suggested that exopolymer-functionalized SeNPs with specific monosaccharide composition and structure could eventually find a potential application as an antioxidant.

Analgesic, Anti-inflammatory, Antipyretic, and In Silico Measurements of Sonneratia caseolaris (L.) Fruits from Sundarbans, Bangladesh.

Sonneratia caseolaris is a widely distributed mangrove plant having much therapeutic importance in traditional medicine. This plant is reported for possessing numerous compounds that are already used for many therapeutic purposes. After finding the presence of antioxidant components in the qualitative antioxidative assay, we went to conduct quantitative tests where the total contents of phenolics, flavonoids, and tannins were estimated as 122 mg GAE/gm, 613 mg QE/gm, and 30 mg GAE/gm, respectively. In DPPH free radical, H2O2, and superoxide radical scavenging assay, the SC50 values were found to be 87, 66, and 192 μg/ml, respectively. In FeCl3 reducing power assay, the RC50 of SC extract and ascorbic acid were 80 and 28 μg/ml, respectively. This extract revealed a significant peripheral analgesic effect in the acetic acid-induced writhing model in mice by reducing the writhing impulse by about 21% and 39% at 250 and 500 mg/kg doses, respectively, and a central analgesic effect in the tail immersion method by elongating the time up to about 22% and 37% at the same doses. In the anti-inflammatory test in mice, this extract reduced the paw edema size over the observed period in a dose-dependent manner. It also showed a significant reduction in the elevated rectal temperature of mice in the observing period in Brewer's yeast-induced pyrexia model. In silico analysis revealed better binding characteristics of ellagic acid and luteolin among other compounds with various receptors that might be responsible for antioxidative and anti-inflammatory properties. From our observation, we suppose that SC fruits might be a potential source of drug leads for various inflammatory disorders.

ASSESSMENT OF INULA CAPPA LEAVES EXTRACTS FOR ANTIDIABETIC POTENTIAL IN EXPERIMENTAL ANIMALS

Diabetes mellitus (DM) is a long-term disease that can be caused by a lack of insulin production by the pancreas, or by the ineffectiveness of the insulin produced. For the study, the antidiabetic effects of methanolic and 50% v/v hydroalcoholic methanolic and extracts of the leaves of Inula cappa were used as oral doses at 100, 200, and 400 mg/kg and Metformine (50 mg/kg) were administered continuously for 21 days as a single morning dose. 18 hours of fasting was used to assess the drug's anti-diabetic effects in normoglycemic rats. On the 0th, 10th, and 21st days of the experiment, glucose oxidase method readings were collected using an autoanalyzer to assess fasting blood glucose levels. Anti-oxidant parameters were determined including, total phenolic content, total flavonoid concentration, DPPH free radical scavenging activity, Hydroxyl radical scavenging activity, Scavenging of Hydrogen Peroxide, Superoxide radical scavenging assay, Nitric oxide scavenging activity and Reducing power assay. The methanolic (ICME) and hydroalcoholic (ICHE) extracts of Inula cappa leaves (100, 200, and 400 mg/kg, p.o.) passes the Oral Glucose Tolerance Test. Both extracts had a greater impact in lowering blood glucose levels. Out of which ICHE at all doses showed significant effect (P<0.05-P<0.001) when compared with control. ICME in terms of glucose tolerance at all doses had significant effects. Keywords: Diabetes mellitus, insulin, metformine, scavenging, Inula cappa.

Evaluation of antioxidant activity of ocimum sanctum

Introduction: Antioxidants are substances that can prevent or slow damage to cells caused by free radicals, unstable molecules that the body produces as a reaction to environmental and other pressures. They are sometimes called “free-radical scavengers.” The sources of antioxidants can be natural or artificial.Periodontitis results from the loss of balance between microbial virulence factors and a proportionate host response.Antioxidant is a substance that is present at low concentrations which significantly delays or prevents oxidation of that substrate.Ocimum sanctum which is a plant extract had a medicinal value and it had been used in asian countries to treat various disease.Ocimum sanctum has an antioxidant agent. Materials and methods: Ocimum Sanctum commercially available powders are used to analyze antioxidant potential. In which three radical scavenging activity analyzed DPPH radical scavenging, Superoxide anion radical scavenging,Nitric oxide radical scavenging. Results: The results from obtained from the reagents shows DPPH radical scavenging activity shows tulsi shows higher activity compared with vitamin c,Superoxide anion radical scavenging,Nitric oxide radical scavenging activity shows vitamin c has higher activity compared with tulsi.

Individual and combined effects of chromium and ultraviolet-B radiation on defense system, ultrastructural changes, and production of secondary metabolite psoralen in a medicinal plant Psoralea corylifolia L.

The present study focuses on the effects of individual and combined stress of chromium (Cr) and ultraviolet-B (UV-B) radiation on Psoralea corylifoliaL. The experiment comprised four sets: (i) control, (ii) eUV-B (elevated UV-B i.e., ambient + 7.2kJm-2day-1 UV-B), (iii) Cr (chromium; 30mgkg-1 soil), and (iv) Cr + eUV-B (chromium and elevated UV-B; Cr 30mgkg-1 and ambient + 7.2kJm-2day-1 UV-B). The eUV-B and Cr individually and in combination showed the variable responses on ultrastructure, physiology and biomass however, the impact was more prominent under individual Cr treatment followed by Cr + eUV-B and eUV-B. Higher bioconcentration factor and the lowered translocation factor consequently led to a higher reduction in the below ground biomass and the lesser reduction in above ground biomass under Cr + eUV-B treatment as compared to individual Cr treatment. In addition, higher induction in the enzymatic (glutathione reductase, ascorbate peroxidase, superoxide dismutase, and glutathione-S-transferase) and non-enzymatic antioxidants (glutathione reduced) were found to be responsible for efficient scavenging of hydrogen peroxide and superoxide radical leading to lowered MDA content under combined treatment as compared to Cr treatment. Deposition of Cr as electron dense granules in the cytoplasm, vacuoles, and cell wall under Cr and Cr + eUV-B is contemplated as one of the cellular mechanisms of P. corylifolia against the toxicity of Cr. Psoralen increased under all treatments with a maximum increase under Cr + eUV-B treatment. Taken together our results accentuated that P. corylifolia can be grown in an area contaminated with Cr and has a higher influx of UV-B for the attainment of psoralen considering its pharmaceutical perspectives.

Oxo-Carotenoids as Efficient Superoxide Radical Scavengers.

Oxo-carotenoids containing conjugated carbonyl groups in their chains were designed to be more efficient superoxide radical scavengers than natural carotenoids, β-carotene and canthaxanthin. A practical chain-extension method for polyene dials (e.g., crocetin dial) was also proposed based on Horner–Wadsworth–Emmons olefination. Double aldol condensation between polyene dials and acetophenones with ring substituents produced oxo-carotenoids with substituted benzene rings. The antioxidant activity of oxo-carotenoids was measured using DPPH (radical) and ABTS (cationic radical) scavenging assays and compared with the analysis with the superoxide (anionic radical) probe. An effective conjugation length by carbon–carbon double bonds is important to provide superior antioxidant activity for oxo-carotenoids, regardless of the type of radical probe used in the assay. Increasing electron density is favorable to strong antioxidant activity in DPPH, and the phenol group is favored in ABTS, whereas electron deficient oxo-carotenoids are very potent in the superoxide radical assay. All oxo-carotenoids exhibited 105~151% better superoxide radical scavenging activity compared to beta-carotene (100%), whereas 38~155% in DPPH and 16~96% in ABTS radical scavenging activities were observed.

Analysis of Antioxidant, Acetylcholinesterase Inhibitory Properties and Chemical Composition of Some Indian Himalayan Species of Berberis: A Comparative Study

Background: Methanolic extracts of the stems of six species of Berberis e.g., Berberis umbellata, B. vulgaris (Syn: B. nepalensis), B. insignis, B. asiatica, and B. aristata were studied for their antioxidant properties and acetylcholinesterase inhibitory properties. Materials and Methods : Antioxidant property was studied in different systems of assay e.g., DPPH radical scavenging assay, superoxide radical scavenging assay, nitric oxide scavenging assay, assay to chelate metal. Acetylcholinesterase (AChE) inhibitory property was measured using AChE from electric eel. Results: It was observed that all the extracts scavenged DPPH, superoxide and nitric oxide radical and chelated metal ion in a dose dependent manner. The antioxidant properties were correlated with total phenol content, total flavonoid content, berberine and palmatine content. The AChE inhibitory activities of the extracts were also correlated well with berberine, palmatine, total phenol and total flavonoid content. A few phenolic compounds were detected by GC-MS. Highest activity in all respect was observed in B. aristata. Conclusion: Methanolic extracts of the stems of B. aristata exhibited the highest antioxidant activity.

Preparation, characterization, and in vitro antioxidant activities of natural selenium-enriched peanut protein fractions

In this work, the content of selenium (Se), physicochemical properties, and antioxidant capacity of Se-enriched peanut proteins isolate (S-PPI) and its fractions arachin (S-Arachin) and conarachin (S-Conarachin) were investigated. The S-PPI, S-Arachin, and S-Conarachin were prepared using natural Se-enriched peanut with alkali extraction, acid precipitation, and sedimentation coefficients method. The Se content of S-PPI (420.83 μg/kg) was two times compared to ordinary peanut protein isolate (O-PPI, 203.10 μg/kg). Besides, the Se is more likely to bind with conarachin than arachin. The solubility curves of these peanut proteins at different pH were similar. The emulsifying activities and the emulsion stability of S-Arachin was relatively low, as well as its foaming activity and the foam stability was the lowest. The DPPH scavenging activity of peanut proteins were decreased in order of S-Conarachin, S-PPI, S-Arachin, and O-PPI, as well as reducing power and the superoxide radical scavenging activity. The antioxidant activity trend was similar to Se content distribution trend, suggesting that the content of Se is related to antioxidant activity. The finding may indicate that Se content played a positive role in promoting the antioxidant activity of peanut protein.

Antioxidant Activity of Fucoidan Modified with Gallic Acid Using the Redox Method.

Antioxidant compounds decrease the amount of intracellular reactive oxygen species (ROS) and, consequently, reduce the deleterious effects of ROS in osteoblasts. Here, we modified a 21 kDa fucoidan (FucA) with gallic acid (GA) using the redox method, to potentiate its antioxidant/protective capacity on pre-osteoblast-like cells (MC3T3) against oxidative stress. The 20 kDa FucA-GA contains 37 ± 3.0 mg GA per gram of FucA. FucA-GA was the most efficient antioxidant agent in terms of total antioxidant capacity (2.5 times), reducing power (five times), copper chelation (three times), and superoxide radical scavenging (2 times). Exposure of MC3T3 cells to H2O2 increased ROS levels and activated caspase-3 along with caspase-9. In addition, the cell viability decreased approximately 80%. FucA-GA also provided the most effective protection against oxidative damage caused by H2O2. Treatment with FucA-GA (1.0 mg/mL) increased cell viability (~80%) and decreased intracellular ROS (100%) and caspase activation (~80%). In addition, Fuc-GA (0.1 mg/mL) abolished H2O2-induced oxidative stress in zebra fish embryos. Overall, FucA-GA protected MC3T3 cells from oxidative stress and could represent a possible adjuvant for the treatment of bone fragility by counteracting oxidative phenomena.

Synthesis, Characterization, and the Antioxidant Activity of Phenolic Acid Chitooligosaccharide Derivatives.

A series of phenolic acid chitooligosaccharide (COS) derivatives synthesized by two mild and green methods were illuminated in this paper. Seven phenolic acids were selected to combine two kinds of COS derivatives: the phenolic acid chitooligosaccharide salt derivatives and the phenolic-acid-acylated chitooligosaccharide derivatives. The structures of the derivatives were characterized by FT-IR and 1H NMR spectra. The antioxidant experiment results in vitro (including DPPH-radical scavenging activity, superoxide-radical scavenging activity, hydroxyl-radical scavenging ability, and reducing power) demonstrated that the derivatives exhibited significantly enhanced antioxidant activity compared to COS. Moreover, the study showed that the phenolic acid chitooligosaccharide salts had stronger antioxidant activity than phenolic-acid-acylated chitooligosaccharide. The cytotoxicity assay of L929 cells in vitro indicated that the derivatives had low cytotoxicity and good biocompatibility. In conclusion, this study provides a possible synthetic method for developing novel and nontoxic antioxidant agents which can be used in the food and cosmetics industry.

Genomic and physiological traits provide insights into ecological niche adaptations of mangrove endophytic Streptomyces parvulus VCCM 22513

PurposeEndophytic Streptomyces parvulus VCCM 22513 isolated from Bruguiera gymnorrhiza in Quang Ninh mangrove forest, northern Vietnam showed abiotic stress tolerance consisting of antioxidant, salt-tolerant, and aromatic-compound degrading activities. The goal of this study was to shed light on genomic bases rendering mangrove endophytic S. parvulus more resilient to environmental stressors.MethodsPhenotypic analysis including antioxidant activities, hydrogen peroxide and sodium chloride resistance, and aromatic compound utilization were evaluated. The genome of strain VCCM 22513 was sequenced using Illumina Miseq sequencing platform and assembled using SPAdes.ResultsOut of 15 endophytic actinomycetes associated with B. gymnorrhiza in Quang Ninh mangrove, northern Vietnam, VCCM 22513 extract showed remarkable antioxidant activities through (1,1-diphenyl-2-picrylhydrazyl) DPPH and superoxide radical scavenging assays of 72.1 ± 0.04% and 38.3 ± 0.16% at 1.6 mg/ml, respectively. The genome consists of a 7,688,855 bp linear chromosome, 6782 protein-coding sequences, and 68 tRNAs. Genomic analysis identified strain VCCM 22513 as Streptomyces parvulus and confirmed a highly conserved core genome and stability of S. parvulus under natural selection. Genome mining revealed the presence of genetic determinants involved in mycothiol and ergothioneine biosynthesis (26 genes), oxidative stress resistance (43 genes), osmoadaptation (87 genes), heat and cold stress (34 genes), aromatic compound degradation (55 genes). Further genome-wide comparison between S. parvulus VCCM 22513 and 11 Streptomyces genomes showed that VCCM 22513 possesses significantly higher copies of genes involved in mycothiol and ergothioneine biosynthesis. In support of this finding, the strain exhibited much resistance to 0.6–1.0 M H2O2 and 6% (w/v) NaCl as compared to Streptomyces cavourensis YBQ59 isolated from Cinnamomum cassia Prels. In addition, the complete pathways for degradation of aromatic compounds including protocatechuate, gentisate, 4-hydroxyphenylpyruvate, cinnamate, 3-phenylpropionate, and styrene were only identified in the genome of VCCM 22513.ConclusionsThe present study revealed for the first time adaptive responses of mangrove endophytic S. parvulus VCCM 22513 to survive in hostile environment. The information shown here provided better understanding of underlying mechanisms related to adaptation and partially plant-microbe interaction of Streptomyces associated with mangrove plants.

Main Bioactive Components and Their Biological Activities from Natural and Processed Rhizomes of Polygonum sibiricum.

Polygonatum sibiricum (Asparagaceae) is often used as an herbal drug in the traditional medicine of Southeast Asia. Its rhizome, called “Huang Jing”, is used in traditional Chinese medicine as an immune system stimulant, hypolipidemic agent, anti-aging agent, anti-fatigue agent, and cardiovascular protectant. We investigated the antioxidant, anti-acetylcholinesterase (AChE), anti-inflammatory, and anti-α-glucosidase effects of various solvent extracts and major bioactive components of Polygonatum sibiricum (PS) and processed Polygonatum sibiricum (PPS). Dichloromethane extract of PS showed stronger antioxidant effects by DPPH, ABTS, and FRAP assays, and EtOAc extract displayed relatively high antioxidant activity by a superoxide radical scavenging test. Moreover, acetone, EtOAc, and dichloromethane extracts displayed a significant anti-α-glucosidase effect. EtOH and CH2Cl2 extracts showed effective AChE inhibitory activity. In addition, dichloromethane extract showed the best inhibition against lipopolysaccharide (LPS)-induced nitric oxide (NO) accumulation in RAW264.7 macrophages. HPLC analysis was used to investigate and compare the content of major active components of various solvent extracts of PS and PPS. Rutin showed the most effective scavenging of DPPH and ABTS free radicals, while scopoletin and isoquercetin displayed the strongest anti-α-glucosidase and anti-AChE effect, respectively. Rutin showed the best inhibition against LPS-induced NO production and also inhibited inducible nitric oxide synthase (iNOS) expression in Western blot. The molecular docking of AChE and iNOS revealed that active components could have a better antagonistic effect than positive controls (common inhibitors). This study shows that the active extracts and components of Polygonatum sibiricum have the potential to be further developed as a natural anti-AChE, anti-α-glucosidase, antioxidant and anti-inflammatory agent.

In vitro Screening for Antioxidant and Antimicrobial Properties of 3,5-Bis(E-thienylmethylene) piperidin-4-one, a Curcumin Analogue

Pharmacognosy Research,2022,14,3,276-283.DOI:10.5530/pres.14.3.40Published:July 2022Type:Original ArticleAuthors:Jayaseelan Nivedha, Kaliyamoorthi Kanimozhi, Subashchandrabose Olikkavi, T. Vidhyasagar, Natesan Vijayakumar, Chinnaiyan Uma, K. Rajeswari, and Lakshmanan Vennila Author(s) affiliations:Jayaseelan Nivedha1, Kaliyamoorthi Kanimozhi1, Subashchandrabose Olikkavi1, T. Vidhyasagar2, Natesan Vijayakumar1, Chinnaiyan Uma4, K. Rajeswari2,3, Lakshmanan Vennila1,* 1Department of Biochemistry and Biotechnology, Annamalai University, Chidambaram, Tamil Nadu, INDIA. 2Department of Chemistry, Annamalai University, Chidambaram, Tamil Nadu, INDIA. 3Department of Chemistry, GAC-CDM, Chidambaram, Tamil Nadu, INDIA. 4Department of Microbiology, Annamalai University, Chidambaram, Tamil Nadu, INDIA. Abstract:Background: Curcumin is a naturally occurring bis-chalcone derivative in the commonly used Indian spice turmeric and is well-known for its potent chemopreventive, anti-angiogenic, anti-cancer properties. 3,5-bis[(E)-thienylmethylene] piperidin-4-one (BTMP) is the newly synthesised synthetic analogue of curcumin that is tested for its antioxidant and antimicrobial properties in vitro. Objectives: This study was to determine the antioxidant activity and antibacterial potentials of newly synthesised analogues of curcumin viz., 3,5-bis[(E)- thienylmethylene] piperidin-4-one (BTMP), was examined in vitro. Materials and Methods: BTMP was evaluated for its antioxidant and antimicrobial using 1,1-diphenyl-2-picryl hydroxyl (DPPH•) radical scavenging assay, 2,2’-azinobis3-ethyl benzothiazoline-6-sulfonic acid (ABTS•+), ferric reducing antioxidant power (FRAP), nitric oxide scavenging assay, superoxide anion radical scavenging assay (O2•−), hydrogen peroxide scavenging, reducing ability assay, metal ion chelating and phosphomolybdenum assays. Results: 40μg/ml of BTMP showed higher antioxidant activity than the other three doses due to its highest free radical scavenging ability at this particular dose. All doses of BTMP showed antimicrobial activity against E. coli and S. aureus. 40μg/ml of BTMP showed the highest zone of inhibition against both tested pathogens. Conclusion: The introduction of basic functionality and the presence of exocyclic double bonds of BTMP has significantly contributed to the antioxidant activity and antimicrobial activity against both gram-positive and gram-negative bacteria. Keywords:Antibacterial, Antioxidant, Curcumin, DPPH, Reducing abilityView:PDF (361.28 KB)

Evaluation Of Antioxidant, Antidiabetic, Anti-Inflammatory And Anticancer Activities Of Delonix Regia Flower Extracts

Non-communicable diseases like diabetes and cancer are the major cause of death worldwide. Various drugs are used for the treatment of these diseases. However, they cause lots of side effects. There is a need for alternate drugs with fewer side effects. Medicinal plants serve as a good source for alternate form of treatment. Therefore, in this study, ethanolic and aqueous extracts of D. regia flowers were evaluated for their antioxidant, antidiabetic, anti-inflammatory and cytotoxic activity to justify its use as a medicinal plant. Total phenol and flavonoid content of the extracts were measured. GC-MS analysis of the extracts were done to investigate the presence of various bioactive compounds. Antioxidant activity was assessed by radical scavenging and reduction assays. Antidiabetic activity was assessed by the ability of extracts to inhibit enzyme alpha amylase. Anti-inflammatory activity was evaluated by membrane stabilization activity. Anticancer activity against MCF-7 and A549 cell lines were measured by the MTT assay.The ethanolic extract contained more phenols (282.940.80 mgGAE/g) and flavonoids (140.912.27 mgQE/g). GC-MS analysis showed the presence of compounds belonging to fatty acids, alkanes, phenols and organic alcohols. The aqueous extract showed strong superoxide radical scavenging activity with a low IC50 of 39.35±0.74 µg/mL. The ethanolic extract showed higher ferric reducing power with an IC50 of 59.65±0.28µg/mL. Ethanolic extract was more potent in inhibiting alpha amylase with a low IC50 value of 47.14±0.6 µg/mL. Ethanolic extract also showed maximum inhibition of 88.86±0.1% against heat induced lysis of cell membrane. Both extracts affected the proliferation of MCF-7 and A549 cell lines at 160 µg/mL. The results of the present study support the use of D. regia flower as a potential source of bioactive phytochemicals and can be used as a plant-based antioxidant, antidiabetic, anti-inflammatory and anticancer agent.